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Completed

NCT Number: NCT03738943

Pyridoxine, P2 Receptor Antagonism, and ATP-mediated Vasodilation in Young Adults

Previous research has identified adenosine triphosphate (ATP) as an important vasodilator that is released from red blood cells during exercise and exposure to hypoxic environments in adult humans. Further, older adults appear to have lower blood flow during both of these stressors and also have lower amounts of ATP released from their red blood cells. However, the contribution of ATP to vasodilation in response to exercise and hypoxia is currently unknown due to the lack of an effective ATP receptor antagonist. We aim to determine whether Vitamin B6 or its metabolite, Pyridoxal-5-Phosphate (PLP) is an effective ATP receptor antagonist.

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Key information

Conditions

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Human Performance and Clinical Research Laboratory

Fort Collins, Colorado, 80523, United States

About this study

Adenosine triphosphate (ATP) is an established vasodilator that is released from red blood cells during a variety of stimuli including exercise and exposure to hypoxic environments. Many studies have shown that infusion of ATP can lead to vasodilation similar to that which is achieved during exercise, and that plasma ATP concentrations increase in a graded fashion during graded exercise. Further, older adults have lower levels of blood flow during exercise and hypoxia compared to their younger counterparts, and the reduced blood flow is coupled with impaired release of ATP from red blood cells during these stimuli. Thus, ATP is believed to be an important vasodilator. However, the role of ATP in the regulation of blood flow is not fully understood due to the lack of an effective ATP receptor (P2Y2) antagonist. Development of an effective P2Y2 antagonist will allow researchers to determine the role of ATP in vasodilation to stimuli such as exercise by comparing blood flow during exercise with and without the blocker. Preliminary data from our laboratory suggests that Vitamin B6 (pyridoxine hydrochloride) or its metabolite Pyridoxal-5-Phosphate (PLP) may be an effective blocker of ATP-mediated vasodilation. As a result, the purpose of this study is to determine whether Vitamin B6 or PLP can inhibit vasodilation in response to intra-arterial infusions of ATP. This study also aims to determine the specificity of Vitamin B6 or PLP by measuring its effect on vasodilation in response to infusion of several other vasodilators.

Participants will be asked to complete one screening visit and one study visit. Once study eligibility has been determined, participants will report to the Human Performance Clinical Research Laboratory at Colorado State University following an overnight fast. A physician will then place a catheter in the brachial artery of the non-dominant arm, and participants will be randomized into one of three study arms to determine which drugs will be infused into the artery. Each arm includes ATP and two other vasodilators. The study will begin by measuring vasodilation in response to four standard doses of each vasodilator. Vasodilation in response to the vasodilators will then be assessed again following infusion of Vitamin B6 or PLP. Reduced vasodilation to any of the drugs during the second trial will suggest that Vitamin B6 or PLP is an antagonist to the channel through which the drug signals. Each study visit will last approximately 4-5 hours.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Sedentary-moderately active
  • Free of chronic disease

Exclusion criteria

  • Current smoker
  • BMI > 29.9 kg/m2
  • Blood pressure equal to or greater than 140/90 mmHg
  • Use of any medications including vitamin B6 supplements or antioxidants

Treatment and study plan

Adenosine triphosphate

Drug

See arm/group descriptions

Other names: ATP

Acetylcholine

Drug

See arm/group descriptions

Other names: Ach

Sodium Nitroprusside

Drug

See arm/group descriptions

Other names: SNP

Adenosine Diphosphate

Drug

See arm/group descriptions

Other names: ADP

Adenosine Monophosphate

Drug

See arm/group descriptions

Other names: AMP

Uridine Triphosphate

Drug

See arm/group descriptions

Other names: UTP

Adenosine

Drug

See arm/group descriptions

Other names: Adenocard

Vitamin B 6

Drug

See arm/group descriptions

Other names: Pyridoxine, Pyridoxine Hydrochloride

Pyridoxal 5'-Phosphate

Drug

See arm/group descriptions

Other names: PLP, P5P, pyridoxal phosphate monohydrate, MC-1

Primary outcomes

  1. Vascular Conductance

    Time frame: Continuous measurement of vascular conductance during the 12 minute dose response for each drug. Measures are repeated following administration of Vitamin B6 or PLP.

    Vascular conductance is an index of vascular tone through which vasodilation can be determined. Vascular conductance is calculated by measuring blood flow in response to infusion of a vasodilator and accounting for blood pressure. Thus, the change in blood flow is due to a change in vascular conductance.

Sponsors and collaborators

Lead sponsor

Colorado State University

Other

Registry information

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Nov 13, 2018
Registry last updated
Jul 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.